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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121016Generated: November 1, 2026

Triphenylphosphine → HCID 21876847, compound

https://huagongshe.com/reaction/2121016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTetrahydro-4H-pyran-4-olHCID 74956—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Hydroxy-4'-nitrobenzophenoneHCID 11096817—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21876847HCID 2187684761.1%

Reaction Steps

Diethyl azodicarboxylate (1.47 g, 8.4 mmol) was slowly added dropwise to a solution of 4-(4-hydroxybenzoyl)-nitrobenzene (1.7 g, 7 mmol) (prepared as described in Example 1, steps), 4-hydroxytetrahydropyran (0.78 g, 7.7 mmol) and triphenylphosphine (2.2 g, 8.4 mmol) in dry tetrahydrofuran (20 mL) while stirring at room temperature under inert atmosphere. The reaction mixture was stirred for an additional hour then quenched with water (1 mL) and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was chromatographed on silica gel (25% ethyl acetate/hexanes) and crystallized from hexanes to give 4-(4-tetrahydropyran-4-yloxybenzoyl)-nitrobenzene (1.4 g, 61%) as a white solid, m.p. 105-106° C.; Analysis for C18H17NO5: Calc.: C, 66.05; H, 5.23; N, 4.28; Found: C, 65.95; H, 5.14; N, 4.38. MS m/e (%): 283 (M+; 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693200B2
Source datasetuspto-grants-2004_02
ORD IDord-182e2d52e17d4a3389210a83656eeda3
Source noteuspto-grants-2004_02